X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
MONDO:0018821Mondo
Findings
No curated finding names X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
90 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Global developmental delayHPOHP:0001263
- Very frequent (80% to 99% of cases)
- Moderate intellectual disabilityHPOHP:0002342
- Very frequent (80% to 99% of cases)
- Abnormal cortical gyrationHPOHP:0002536
- Frequent (30% to 79% of cases)
- Abnormality of the eyeHPOHP:0000478
- Frequent (30% to 79% of cases)
- Abnormality of the genitourinary systemHPOHP:0000119
- Frequent (30% to 79% of cases)
- Anal atresiaHPOHP:0002023
- Frequent (30% to 79% of cases)
- Choanal atresiaHPOHP:0000453
- Frequent (30% to 79% of cases)
- Dandy-Walker malformationHPOHP:0001305
- Frequent (30% to 79% of cases)
- Depigmentation/hyperpigmentation of skinHPOHP:0007483
- Frequent (30% to 79% of cases)
- Floppy infantHPOHP:0008947
- Frequent (30% to 79% of cases)
- Hypoplasia of the corpus callosumHPOHP:0002079
- Frequent (30% to 79% of cases)
- Postaxial polydactylyHPOHP:0100259
- Frequent (30% to 79% of cases)
Show the remaining 78
- Short statureHPOHP:0004322
- Frequent (30% to 79% of cases)
- 1-minute APGAR score of 1HPOHP:0030928
- Occasional (5% to 29% of cases)
- 5-minute APGAR score of 5HPOHP:0030925
- Occasional (5% to 29% of cases)
- Abnormal abdominal wall morphologyHPOHP:0004298
- Occasional (5% to 29% of cases)
- Abnormal circulating thyroid hormone concentrationHPOHP:0031508
- Occasional (5% to 29% of cases)
- Abnormal periodontium morphologyHPOHP:0410026
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- USP9XHGNC:12632
- Supportive · Orphanet · X-linked · 2021
Where it sits
- A kind of
Other names
2 names
Resolves to: X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability
- Also called
- X-linked facial dysmorphism-short stature-choanal atresia-intellectual disability syndrome limited to femalesX-linked facial dysmorphism-short stature-choanal atrsia-intellectual disability syndrome limited to females